| Common Name |
Diazenedicarboxamide
| Description |
Bleaching agent for flourDiazenedicarboxamide belongs to the family of Azo Compounds. These are derivatives ofA diazene(diimide), HN=NH, wherein both hydrogens are substituted by hydrocarbyl groups, e.g. PhN=NPhA azobenzeneA or diphenyldiazene[1]. (Reference: [1] IUPAC. Compendium of Chemical Terminology, 2nd ed. (the “Gold Book”). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. doi:10.1351/goldbook. (PAC, 1995, 67, 1307 (Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)) on page 1321)).
| Structure |
MOLSDF3D-SDFPDBSMILESInChI View 3D Structure
Structure for HMDB29616 (Diazenedicarboxamide)
| Synonyms |
| Value |
Source |
1,1'-AzobiscarbamideHMDB
1,1'-Azobis[formamide]HMDB
1,1'-AzodiformamideHMDB
AZM 2SHMDB
Azobis ca 110bHMDB
Azobis ca 51CHMDB
AzobiscarbonamideHMDB
AzobiscarboxamideHMDB
AzobisformamideHMDB
AzocelHMDB
AzodicarbamideHMDB
AzodicarboamideHMDB
AzodicarbonamideHMDB
AzodicarboxamideHMDB
Azodicarboxylic acid diamideHMDB
AzodiformamideHMDB
Azoform aHMDB
AzoformamideHMDB
AzoplastoneHMDB
Celogen azHMDB
EviporHMDB
Genitron epcHMDB
Paramid K1HMDB
VinyforHMDB
1,1-AzobisformamideMeSH
| Chemical Formlia |
C2H4N4O2
| Average Molecliar Weight |
116.0788
| Monoisotopic Molecliar Weight |
116.033425392
| IUPAC Name |
(E)-N-[(C-hydroxycarbonimidoyl)imino]carbamimidic acid
| Traditional Name |
azodicarbonamide
| CAS Registry Number |
123-77-3
| SMILES |
OC(=N)N=NC(O)=N
| InChI Identifier |
InChI=1S/C2H4N4O2/c3-1(7)5-6-2(4)8/h(H2,3,7)(H2,4,8)/b6-5+
| InChI Key |
XOZUGNYVDXMRKW-AATRIKPKSA-N
| Chemical Taxonomy |
| Description |
This compound belongs to the class of chemical entities known as azo compounds. These are derivatives of diazene(diimide), HN=NH, wherein both hydrogens are substituted by hydrocarbyl groups, e.g. PhN=NPh azobenzene or diphenyldiazene.
| Kingdom |
Chemical entities
| Super Class |
Organic compounds
| Class |
Organic nitrogen compounds
| Sub Class |
Organonitrogen compounds
| Direct Parent |
Azo compounds
| Alternative Parents |
Propargyl-type 1,3-dipolar organic compounds
Carboximidic acids and derivatives
Organopnictogen compounds
Organooxygen compounds
Imines
Hydrocarbon derivatives
| Substituents |
Azo compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidic acid derivative
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Imine
Aliphatic acyclic compound
| Molecliar Framework |
Aliphatic acyclic compounds
| External Descriptors |
Not Available
| Ontology |
| Status |
Expected but not Quantified
| Origin |
Food
| Biofunction |
Not Available
| Application |
Nutrient
| Cellliar locations |
Cytoplasm
Extracellliar
| Physical Properties |
| State |
Not Available
| Experimental Properties |
| Property |
Value |
Reference |
Melting Point225 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.035 mg/mL at 20 °CNot Available
LogP-1.70Not Available
| Predicted Properties |
| Property |
Value |
Source |
Water Solubility3.93 mg/mLALOGPS
logP-1ALOGPS
logP-0.51ChemAxon
logS-2.5ALOGPS
pKa (Strongest Acidic)3.04ChemAxon
pKa (Strongest Basic)1.93ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area112.88 Å2ChemAxon
Rotatable Bond Count0ChemAxon
Refractivity45.36 m3·mol-1ChemAxon
Polarizability9.48 Å3ChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rlie of FiveYesChemAxon
Ghose FilterYesChemAxon
Vebers RlieYesChemAxon
MDDR-like RlieYesChemAxon
| Spectra |
| Spectra |
| Spectrum Type |
Description |
Splash Key |
|
| Predicted LC-MS/MS |
Predicted LC-MS/MS Spectrum – 10V, PositiveNot Available
| Predicted LC-MS/MS |
Predicted LC-MS/MS Spectrum – 20V, PositiveNot Available
| Predicted LC-MS/MS |
Predicted LC-MS/MS Spectrum – 40V, PositiveNot Available
| Predicted LC-MS/MS |
Predicted LC-MS/MS Spectrum – 10V, NegativeNot Available
| Predicted LC-MS/MS |
Predicted LC-MS/MS Spectrum – 20V, NegativeNot Available
| Predicted LC-MS/MS |
Predicted LC-MS/MS Spectrum – 40V, NegativeNot Available
| Biological Properties |
| Cellliar Locations |
Cytoplasm
Extracellliar
| Biofluid Locations |
Not Available
| Tissue Location |
Not Available
| Pathways |
Not Available
| Normal Concentrations |
| Not Available |
| Abnormal Concentrations |
|
Not Available
| Associated Disorders and Diseases |
| Disease References |
None
| Associated OMIM IDs |
None
| External Links |
| DrugBank ID |
Not Available
| DrugBank Metabolite ID |
Not Available
| Phenol Explorer Compound ID |
Not Available
| Phenol Explorer Metabolite ID |
Not Available
| FoodDB ID |
FDB000784
| KNApSAcK ID |
Not Available
| Chemspider ID |
4575589
| KEGG Compound ID |
Not Available
| BioCyc ID |
Not Available
| BiGG ID |
Not Available
| Wikipedia Link |
Not Available
| NuGOwiki Link |
HMDB29616
| Metagene Link |
HMDB29616
| METLIN ID |
Not Available
| PubChem Compound |
5462814
| PDB ID |
Not Available
| ChEBI ID |
Not Available
Product: SKI II
References |
| Synthesis Reference |
Not Available |
| Material Safety Data Sheet (MSDS) |
Not Available |
| General References |
- (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
|
PMID: 25933382